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Prenatal and postnatal evaluation of polymicrogyria with band heterotopia

The coexistence of band heterotopia and polymicrogyria is extremely rare though it has been reported in the presence of corpus callosum anomalies and megalencephaly. We present prenatal and postnatal MRI findings of a rare case of diffuse cortical malformation characterized by polymicrogyria and ban...

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Autores principales: Nagaraj, Usha D., Hopkin, Robert, Schapiro, Mark, Kline-Fath, Beth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5551996/
https://www.ncbi.nlm.nih.gov/pubmed/28828134
http://dx.doi.org/10.1016/j.radcr.2017.04.007
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author Nagaraj, Usha D.
Hopkin, Robert
Schapiro, Mark
Kline-Fath, Beth
author_facet Nagaraj, Usha D.
Hopkin, Robert
Schapiro, Mark
Kline-Fath, Beth
author_sort Nagaraj, Usha D.
collection PubMed
description The coexistence of band heterotopia and polymicrogyria is extremely rare though it has been reported in the presence of corpus callosum anomalies and megalencephaly. We present prenatal and postnatal MRI findings of a rare case of diffuse cortical malformation characterized by polymicrogyria and band heterotopia. Agenesis of the corpus callosum and megalencephaly were also noted. In addition, bilateral closed-lip schizencephaly was identified on postnatal MRI, which has not been previously reported with this combination of imaging findings. Polymicrogyria with band heterotopia can occur and can be diagnosed with fetal MRI. The coexistence of corpus callosum anomalies and megalencephaly comprises a rare phenotype that has been previously described, suggesting an underlying genetic abnormality.
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spelling pubmed-55519962017-08-21 Prenatal and postnatal evaluation of polymicrogyria with band heterotopia Nagaraj, Usha D. Hopkin, Robert Schapiro, Mark Kline-Fath, Beth Radiol Case Rep Case Report The coexistence of band heterotopia and polymicrogyria is extremely rare though it has been reported in the presence of corpus callosum anomalies and megalencephaly. We present prenatal and postnatal MRI findings of a rare case of diffuse cortical malformation characterized by polymicrogyria and band heterotopia. Agenesis of the corpus callosum and megalencephaly were also noted. In addition, bilateral closed-lip schizencephaly was identified on postnatal MRI, which has not been previously reported with this combination of imaging findings. Polymicrogyria with band heterotopia can occur and can be diagnosed with fetal MRI. The coexistence of corpus callosum anomalies and megalencephaly comprises a rare phenotype that has been previously described, suggesting an underlying genetic abnormality. Elsevier 2017-05-27 /pmc/articles/PMC5551996/ /pubmed/28828134 http://dx.doi.org/10.1016/j.radcr.2017.04.007 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Nagaraj, Usha D.
Hopkin, Robert
Schapiro, Mark
Kline-Fath, Beth
Prenatal and postnatal evaluation of polymicrogyria with band heterotopia
title Prenatal and postnatal evaluation of polymicrogyria with band heterotopia
title_full Prenatal and postnatal evaluation of polymicrogyria with band heterotopia
title_fullStr Prenatal and postnatal evaluation of polymicrogyria with band heterotopia
title_full_unstemmed Prenatal and postnatal evaluation of polymicrogyria with band heterotopia
title_short Prenatal and postnatal evaluation of polymicrogyria with band heterotopia
title_sort prenatal and postnatal evaluation of polymicrogyria with band heterotopia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5551996/
https://www.ncbi.nlm.nih.gov/pubmed/28828134
http://dx.doi.org/10.1016/j.radcr.2017.04.007
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